Method for preparing skin surface and determining glucose levels from that surface

ABSTRACT

This involves a non-invasive glucose measurement device and a process for determining blood glucose level in the human body using the device. In typical operation, the glucose measurement device is self-normalizing in that it does not employ an independent reference sample in its operation. The device uses attenuated total reflection (ATR) infrared spectroscopy. Preferably, the device is used on a fingertip and compares two specific regions of a measured infrared spectrum to determine the blood glucose level of the user. Clearly, this device is especially suitable for monitoring glucose levels in the human body, and is especially beneficial to users having diabetes mellitus. The device and procedure may be used for other analyte materials which exhibit unique mid-IR signatures of the type described herein and that are found in appropriate regions of the outer skin.

RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.09/547,433, entitled “Infrared ATR glucose measurement system (II)”,filed on Apr. 12, 2000, which was a continuation-in-part ofPCT/US99/23823, filed Oct. 12, 1999, designating the U.S., which in turnderives benefit from U.S. app. Ser. No. 60/103,883, to Berman and Roe,filed Oct. 13, 1998.

FIELD OF THE INVENTION

This invention involves a non-invasive glucose measurement device and aprocess for determining blood glucose level in the human body using thedevice. In typical operation, the glucose measurement device isself-normalizing in that it does not employ an independent referencesample in its operation.; The inventive device uses attenuated totalreflection (ATR) infrared spectroscopy. Preferably, the device is usedon a fingertip or other part of the body. Although the inventiveprocedure preferably compares two specific regions of a measuredmid-infrared spectrum to determine the blood glucose level of the user.Clearly, this device is especially suitable for monitoring glucoselevels in the human body, and is especially beneficial to users havingdiabetes mellitus. The device and procedure may be used for othermaterials which exhibit unique mid-IR signatures of the type describedbelow and that are found in appropriate regions of the outer skin. Acleaning kit and related procedure for preparation of the skin surfaceis also included.;

BACKGROUND OF THE INVENTION

The American Diabetes Association reports that nearly 6% of thepopulation in the United States, a group of 16 million people, hasdiabetes. The Association further reports that diabetes is the seventhleading cause of death in the United States, contributing to nearly200,000 deaths per year. Diabetes is a chronic disease having no cure.The complications of the disease include blindness, kidney disease,nerve disease, and heart disease, perhaps with stroke. Diabetes is saidto be the leading cause of new cases of blindness in individuals in therange of ages between 20 and 74; from 12,000-24,000 people per year losetheir sight because of diabetes. Diabetes is the leading cause ofend-stage renal disease, accounting for nearly 40% of new cases. Nearly60-70% of people with diabetes have mild to severe forms of diabeticnerve damage which, in severe forms, can lead to lower limb amputations.People with diabetes are 2-4 times more likely to have heart disease andto suffer strokes.

Diabetes is a disease in which the body does not produce or properly useinsulin, a hormone needed to convert sugar, starches, and the like intoenergy. Although the cause of diabetes is not completely understood,genetics, environmental factors, and viral causes have been partiallyidentified.

There are two major types of diabetes: Type I and Type II. Type Idiabetes (formerly known as juvenile diabetes) is an autoimmune diseasein which the body does not produce any insulin and most often occurs inyoung adults and children. People with Type I diabetes must take dailyinsulin injections to stay alive.

Type II diabetes is a metabolic disorder resulting from the body'sinability to make enough, or properly to use, insulin. Type II diabetesaccounts for 90-95% of diabetes. In the United States, Type II diabetesis nearing epidemic proportions, principally due to an increased numberof older Americans and a greater prevalence of obesity and a sedentarylifestyle.

Insulin, in simple terms, is the hormone that unlocks the cells of thebody, allowing glucose to enter those cells and feed them. Since, indiabetics, glucose cannot enter the cells, the glucose builds up in theblood and the body's cells literally starve to death.

Diabetics having Type I diabetes typically are required toself-administer insulin using, e.g., a syringe or a pin with needle andcartridge. Continuous subcutaneous insulin infusion via implanted pumpsis also available. Insulin itself is typically obtained from porkpancreas or is made chemically identical to human insulin by recombinantDNA technology or by chemical modification of pork insulin. Althoughthere are a variety of different insulins for rapid-, short-,intermediate-, and long-acting forms that may be used variously,separately or mixed in the same syringe, use of insulin for treatment ofdiabetes is not to be ignored.

It is highly recommended by the medical profession that insulin-usingpatients practice self-monitoring of blood glucose (SMBG). Based uponthe level of glucose in the blood, individuals may make insulin dosageadjustments before injection. Adjustments are necessary since bloodglucose levels vary day to day for a variety of reasons, e.g., exercise,stress, rates of food absorption, types of food, hormonal changes(pregnancy, puberty, etc.) and the like. Despite the importance of SMBG,several studies have found that the proportion of individuals whoself-monitor at least once a day significantly declines with age. Thisdecrease is likely due simply to the fact that the typical, most widelyused, method of SMBG involves obtaining blood from a finger stick. Manypatients consider obtaining blood to be significantly more painful thanthe self-administration of insulin.

There is a desire for a less invasive method of glucose measurement.Methods exist or are being developed for a minimally invasive glucosemonitoring, which use body fluids other than blood (e.g., sweat orsaliva), subcutaneous tissue, or blood measured less invasively. Sweatand saliva are relatively easy to obtain, but their glucoseconcentration appears to lag in time significantly behind that of bloodglucose. Measures to increase sweating have been developed and seem toincrease the timeliness of the sweat glucose measurement, however.

Subcutaneous glucose measurements seem to lag only a few minutes behinddirectly measured blood glucose and may actually be a better measurementof the critical values of glucose concentrations in the brain, muscle,and in other tissue. Glucose may be measured by non-invasive orminimally-invasive techniques, such as those making the skin or mucousmembranes permeable to glucose or those placing a reporter molecule inthe subcutaneous tissue. Needle-type sensors have been improved inaccuracy, size, and stability and may be placed in the subcutaneoustissue or peripheral veins to monitor blood glucose with smallinstruments. See, “An Overview of Minimally Invasive Technologies”,Clin. Chem. 1992 September; 38(9):1596-1600.

Truly simple, non-invasive methods of measuring glucose are notcommercially available.

U.S. Pat. No. 4,169,676 to Kaiser, shows a method for the use of ATRglucose measurement by placing the ATR plate directly against the skinand especially against the tongue. The procedure and device shown thereuses a laser and determines the content of glucose in a specific livingtissue sample by comparing the IR absorption of the measured materialagainst the absorption of IR in a control solution by use of a referenceprism. See, column 5, lines 31 et seq.

Swiss Patent No. 612,271, to Dr. Nils Kaiser, appears to be the Swisspatent corresponding to U.S. Pat. No. 4,169,676.

U.S. Pat. No. 4,655,255, to Dähne et al., describes an apparatus fornon-invasively measuring the level of glucose in a blood stream ortissues of patients suspected to have diabetes. The method isphotometric and uses light in the near-infrared region. Specifically,the procedure uses light in the 1,000 to 2,500 nm range. Dähne's deviceis jointly made up to two main sections, a light source and a detectorsection. They may be situated about a body part such as a finger. Thedesired near-infrared light is achieved by use of filters. The detectorsection is made up of a light-collecting integrating sphere orhalf-sphere leading to a means for detecting wavelengths in thenear-infrared region. Dähne et al. goes to some lengths teaching awayfrom the use of light in the infrared range having a wavelength greaterthan about 2.5 micrometers since those wavelengths are strongly absorbedby water and have very little penetration capability into living tissuescontaining glucose. That light is said not to be “readily useable toanalyze body tissue volumes at depths exceeding a few microns or tens ofmicrons.” Further, Dähne et al. specifically indicates that an ATRmethod which tries to circumvent the adverse consequences of the heateffect by using a total internal reflection technique is able only toinvestigate to tissue depths not exceeding about 10 micrometers, a depthwhich is considered by Dähne et al. to be “insufficient to obtainreliable glucose determination information.”

U.S. Pat. No. 5,028,787, to Rosenthal et al., describes a non-invasiveglucose monitoring device using near-infrared light. The light is passedinto the body in such a way that it passes through some blood-containingregion. The so-transmitted or reflected light is then detected using anoptical detector. The near-infrared light sources are preferablyinfrared emitting diodes (IRED). U.S. Pat. No. 5,086,229 is acontinuation in part of U.S. Pat. No. 5,028,787.

U.S. Pat. No. 5,178,142, to Harjunmaa et al, teaches the use of astabilized near-infrared radiation beam containing two alternatingwavelengths in a device to determine a concentration of glucose or otherconstituents in a human or animal body. Interestingly, one of thetransmitted IR signals is zeroed by variously tuning one of thewavelengths, changing the extracellular to intracellular fluid ratio ofthe tissue by varying the mechanical pressure on a tissue. Or, the ratiomay be allowed to change as a result of natural pulsation, e.g., byheart rate. The alternating component of the transmitted beam ismeasured in the “change to fluid ratio” state. The amplitude of thevarying alternating signal is detected and is said to represent glucoseconcentration or is taken to represent the difference in glucoseconcentration from a preset reference concentration.

U.S. Pat. No. 5,179,951 and its divisional, U.S. Pat. No. 5,115,133, toKnudson, show the application of infrared light for measuring the levelof blood glucose in blood vessels in the tympanic membrane. The detectedsignal is detected, amplified, decoded, and, using a microprocessor,provided to a display device. The infrared detector (No. 30 in thedrawings) is said simply to be a “photo diode and distance signaldetector” which preferably includes “means for detecting the temperatureof the volume in the ear between the detector and the ear's tympanicmembrane.” Little else is said about the constituency of that detector.

U.S. Pat. No. 5,433,197, to Stark, describes a non-invasive glucosesensor. The sensor operates in the following fashion. A near-infraredradiation is passed into the eye through the cornea and the aqueoushumor, reflected from the iris or the lens surface, and then passed outthrough the aqueous humor and cornea. The reflected radiation iscollected and detected by a near-infrared sensor which measures thereflected energy in one or more specific wavelength bands. Comparison ofthe reflected energy with the source energy is said to provide a measureof the spectral absorption by the eye components. In particular, it issaid that the level of glucose in the aqueous humor is a function of thelevel of glucose in the blood. It is said in Stark that the measuredglucose concentration in the aqueous humor tracks that of the blood by afairly short time, e.g., about 10 minutes. The detector used ispreferably a photodiode detector of silicon or InGaAs. The infraredsource is said preferably to be an LED, with a refraction grating sothat the light of a narrow wavelength band, typically 10 to 20nanometers wide, passes through the exit slit. The light is in thenear-infrared range. The use of infrared regions below 1400 nanometersand in the region between 1550 and 1750 nanometers is suggested.

U.S. Pat. No. 5,267,152, to Yang et al., shows a non-invasive method anddevice for measuring glucose concentration. The method and apparatususes near-infrared radiation, specifically with a wavelength of 1.3micrometers to 1.8 micrometers from a semiconductor diode laser. Theprocedure is said to be that the light is then transmitted down throughthe skin to the blood vessel where light interacts with variouscomponents of the blood and is then diffusively reflected by the bloodback through the skin for measurement.

Similarly, U.S. Pat. No. 5,313,941, to Braig et al., suggests aprocedure and apparatus for monitoring glucose or ethanol and otherblood constituents in a non-invasive fashion. The measurements are madeby monitoring absorption of certain constituents in the longer infraredwavelength region. The long wavelength infrared energy is passed throughthe finger or other vascularized appendage. The infrared light passingthrough the finger is measured. The infrared source is pulsed to preventburning or other patient discomfort. The bursts are also synchronizedwith the heartbeat so that only two pulses of infrared light are sentthrough the finger per heartbeat. The detected signals are then analyzedfor glucose and other blood constituent information.

U.S. Pat. No. 5,398,681, to Kuperschmidt, shows a device which is saidto be a pocket-type apparatus for measurement of blood glucose using apolarized-modulated laser beam. The laser light is introduced into afinger or ear lobe and the phase difference between a reference signaland the measurement signal is measured and processed to formulate andcalculate a blood glucose concentration which is then displayed.

U.S. Pat. No. 6,001,067 shows an implantable device suitable for glucosemonitoring. It utilizes a membrane which is in contact with a thinelectrolyte phase, which in turn is covered by an enzyme-containingmembrane, e.g., glucose oxidase in a polymer system. Sensors arepositioned in such a way that they measure the electrochemical reactionof the glucose within the membranes. That information is then passed tothe desired source.

None of the cited prior art suggests the device and method of using thisdevice described and claimed below.

SUMMARY OF THE INVENTION

This invention is a glucose level measurement device utilizing IR-ATRspectroscopy and a method of using the device. The inventive deviceitself is preferably made up of four parts:

a.) an IR source for emitting an IR beam into the ATR plate,

b.) the ATR plate against which the sampled human skin surface ispressed, and

c.) at least two IR sensors for simultaneously measuring absorbance oftwo specific regions of the IR spectrum, i.e., a “referencingwavelength” and a “measuring wavelength.” The IR source must emit IRradiation at least in the region of the referencing wavelength and themeasuring wavelength. For glucose, the referencing wavelength is betweenabout 8.25 micrometers and about 8.75 micrometers and the measuringwavelength is between about 9.50 micrometers and about 10.00micrometers. The IR sources may be broadband IR sources, non-lasersources, or two or more selected wavelength lasers.

Other analyte materials which have both referencing wavelengths andmeasuring wavelengths as are described in more detail below and thatpreferably are found in the outer regions of the skin may be measuredusing the inventive devices and procedures described herein.

The ATR plate is configured to permit multiple internal reflections,perhaps 3-15 internal reflections or more, against said measurementsurface prior to measurement by the IR sensors. Typically the IR beamemitted from the ATR plate is split for the IR sensors using a beamsplitter or equivalent optical device. Once the split beams are measuredby the IR sensors, the resulting signals are then transformed usinganalog comparators or digital computers into readable or displayablevalues.

It is usually important that the device have some accommodation forholding the body part against the ATR plate, preferably at some valuewhich is constant and above a selected minimum pressure.

The method for determining the blood glucose level, using the glucosemeasurement device, comprises the steps of.

a.) contacting a selected skin surface with the ATR plate,

b.) irradiating that human skin surface with an IR beam havingcomponents at least in the region of the referencing wavelength and themeasuring wavelength, and

c.) detecting and quantifying those referencing and said measuringwavelength components in that reflected IR beam.

The procedure ideally includes the further steps of maintaining the skinsurface on said ATR plate at an adequate pressure which is both constantand above a selected minimum pressure and, desirably cleaning the skinsurface before measurement. A step of actually measuring the pressuremay also be included.

A normalizing step practiced by simultaneously detecting and quantifyingthe referencing and measuring wavelength components prior to contactingthe skin surface is also desirable.

A final portion of this invention is a cleaning kit used for cleaningthe object skin prior to testing and a process of using that kit. Thekit usually is made up of sealed packets, preferably containingabsorbent pads, of:

a.) a glucose solvent, e.g., water and/or other highly polar solvent andperhaps containing a weak acid,

b.) a solvent for removing the glucose solvent, e.g., isopropanol, and

c.) a skin softener or pliability enhancer, e.g., various mineral oilssuch as “Nujol”, not having significant IR wavelength peaks betweenabout 8.25 micrometers and about 8.75 micrometers or between about 9.50micrometers and about 10.00 micrometers. I prefer to mix components b.)and c.). The solvent for removing the glucose solvent similarly shouldnot have an interfering IR signal which persists after several minutes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A, 1B, 1C, and 1D show a side view of various ATR plates andtheir general operation.

FIG. 2 shows an IR spectrum of d-glucose.

FIG. 3 shows a schematicized layout of the optics of the inventivedevice.

FIG. 4 shows a packaged variation of the inventive glucose measuringdevice.

FIG. 5 shows a graph of pressure on the ATR crystal vs. IR value.

FIG. 6 shows a graph correlating glucose levels measured using aspecific variation of the device with glucose levels in the blooddetermined using a commercial device.

FIG. 7 shows a graph using a transmittance trough as the referencingwavelength.

FIG. 8 shows a pair of glucose IR curves (taken before and after eating)for an individual having diabetes made using the inventive glucosemeasuring device.

FIG. 9 shows a graph comparing glucose levels in a non-diabeticindividual (taken before and after eating) made using the inventiveglucose measuring device and direct blood measurement. This graph showsthat the inventive procedure tracks blood glucose levels with minimumtime lag.

DESCRIPTION OF THE INVENTION

The device in this invention uses infrared (“IR”) attenuated totalreflectance (“ATR”) spectroscopy to detect and ultimately to determinethe level of a selected analyte, preferably blood glucose, in the humanbody. Preferably, the inventive device uses an ATR procedure in whichthe size and configuration of the crystal permits a number of internalreflections before the beam is allowed to exit the crystal with itsmeasured information. In general, as shown in FIGS. 1A and 1B, when aninfrared beam (102) is incident on the upper surface of the ATR crystal(104)—or ATR plate—at an angle which exceeds a critical angle Θ_(C), thebeam (102) will be completely totally reflected within crystal (104).Each reflection of the beam within the ATR plate, and specificallyagainst the upper surface (114), provides a bit more information aboutthe composition of the sample (112) resting against that upper surface(114). The more numerous the reflections, and the greater thepenetration depth of the reflection, the higher is the quality of theinformation. The incident beam (102) becomes reflected beam (106) as itexits crystal (104) as shown in FIG. 1A. Higher refractive indexmaterials are typically chosen for the ATR crystal to minimize thecritical angle. The critical angle is a function of the refractiveindices of both the sample and the ATR crystal and is defined as:$\Theta_{C} = {\sin^{- 1}\left( \frac{n_{2}}{n_{1}} \right)}$

Here, n₁ is the refractive index of the ATR crystal and n₂ is therefractive index of the sample.

Throughout this specification, we refer to wavelength measures asspecific values. It should be understood that we intend those values tobe bands or ranges of values, typically with a tolerance of +/−0.20micron, preferably +/−0.10 micron. For instance, a value of 8.25 micronswould mean a band of 8.15 to 8.35 microns, and perhaps 8.05 to 8.45microns depending upon the context.

As shown in FIG. 1B, the internally reflected beam (108) includes anevanescent wave (110) which penetrates a short distance into sample(112) over a wide wavelength range. In those regions of the IR spectrumin which the sample absorbs IR, some portion of the light does notreturn to the sensor. It is these regions of IR absorbance which provideinformation, in this inventive device, for quantification of the glucoselevel.

We have found that the mid-IR spectrum does not penetrate into the skinto an appreciable level. Specifically, the skin is made up of a numberof layers: the outermost—the stratum corneum—is a layer substantiallyfree of cholesterol, water, gamma globulin, albumin, and blood. It is ashallow outer region covering the stratum granulosum, the stratumspinosum, and the basal layer. The area between the basal layer to theoutside is not vascularized. It is unlikely that any layer other thanthe stratum corneum is traversed by the mid-IR light involved in thisinventive device. Although we do not wish to be bound by theory, it islikely that the eccrine or sweat glands transport the glucose to theouter skin layers for measurement and analysis by our inventions.

We prefer the use of higher refractive index crystals such as zincselenide, zinc sulfide, diamond, germanium, and silicon as the ATRplate. The index of refraction of the ATR plate (104) should besignificantly higher than that of the sample (112).

Further, the ATR crystal (104) shown in FIG. 1A is shown to betrapezoidal and having an upper surface (114) for contact with thesample, which sample, in this case, is skin from a living human body.However, this shape is only for the purposes of mechanical convenienceand ease of application into a working commercial device. Other shapes,in particular, a parallelogram (111) such as shown in FIG. 1C and thereflective crystal (113) shown in FIG. 1D having mirrored end (115), arealso quite suitable for this inventive device should the designer sorequire. The mirrored reflective crystal (113) has the advantage of, andperhaps the detriment of having both an IR source and the IR sensors atthe same end of the crystal.

It is generally essential that the ATR crystal or plate (104) have asample or upper surface (114) which is essentially parallel to the lowersurface (116). In general, the ATR plate (104) is preferably configuredand utilized so that the product of the practical number of internalreflections of internal reflected beam (108) and the skin penetrationper reflection of this product is maximized. When maximizing thisproduct, called the effective pathlength (EPL), the information level inbeam (106) as it leaves ATR plate (104) is significantly higher.Further, the higher the value of the index of refraction, n₂, of the ATRplate (104), the higher is the number of internal reflections. Thesensitivity of the IR sensors also need not be as high when the EPL ismaximized. We consider the number of total reflections within thecrystal to be preferably from 3-15 or more for adequate results.

We have surprisingly found that a glucose measuring device madeaccording to this invention is quite effective on the human skin of thehands and fingers. We have found that the glucose concentration asmeasured by the inventive devices correlates very closely with theglucose concentration determined by a direct determination from a bloodsample. As will be discussed below, the glucose level as measured by theinventive device also is surprisingly found closely to track the glucoselevel of blood in time as well. This is surprising in that the IR beamlikely passes into the skin, i.e., the stratum corneum, for only a fewmicrons. It is unlikely in a fingertip that any blood is crossed by thatlight path. As discussed above, the stratum corneum is the outer layerof skin and is substantially unvascularized. The stratum corneum is thefinal outer product of epidermal differentiation or keratinization. Itis made up of a number of closely packed layers of flattened polyhedralcorneocytes (also known as squames). These cells overlap and interlockwith neighboring cells by ridges and grooves. In the, thin skin of thehuman body, this layer may be only a few cells deep, but in thickerskin, such as may be found on the toes and feet, it may be more than 50cells deep. The plasma membrane of the corneocyte appears thickenedcompared with that of keratinocytes in the lower layers of the skin, butthis apparent deposition of a dense marginal band formed bystabilization of a soluble precursor, involucrin, just below the stratumcorneum.

It is sometimes necessary to clean the skin exterior prior beforesampling to remove extraneous glucose from the skin surface. When doingso, it is important to select cleaning materials which have IR spectrathat do not interfere with the IR spectra of glucose. We consider a kitof the following to be suitable for preparation of the sample skin forthe testing. The components are: a.) a glucose solvent, e.g., water orother highly polar solvent; b.) a solvent for removing the water, e.g.,isopropanol, and c.) a skin softener or pliability enhancer not havingsignificant IR peaks in the noted IR regions, e.g., mineral oils such asthose sold as “Nujol”. Preferably the b.) and c.) components areadmixed, although they need not be. Certain mixtures of the first twocomponents may be acceptable, but only if the sampling situation is suchthat the solvents evaporate without spectrographically significantresidue. We have also found that soap and its residue are sometimes aproblem. Consequently, addition of a weak acid again not havingsignificant IR peaks in the noted IR regions, to the a.) component,i.e., the solvent for removing glucose, is desirable. The preferred weakacid is boric acid. The inventive kit preferably is made up of sealedpackets of the components, most preferably each packet containing anabsorbent pad.

Additionally, the inventive device can be highly simplified compared toother known devices in that the device can be “self-normalizing” due tothe specifics of the IR signature of glucose. FIG. 2 shows the IRabsorbance spectra of d-glucose. The family of curves there shows thatin certain regions of the IR spectrum, there is a correlation betweenabsorbance and the concentration of glucose. Further, there is a regionin which the absorbance is not at all dependent upon the concentrationof glucose. Our device, in its preferable method of use, uses these tworegions of the IR spectra. These regions are in the so-called mid-IRrange, i.e., wavelengths between 2.5 and 14 micrometers. In particular,the “referencing wavelength” point is just above 8 micrometers (150),e.g., 8.25 to 8.75 micrometers, and the pronounced peaks (152) at theregion between about 9.50 and 10.00 micrometers is used as a “measuringwavelength”. The family of peaks (152) may be used to determine thedesired glucose concentration.

Use of the two noted IR regions is also particularly suitable sinceother components typically found in the skin, e.g., water, cholesterol,etc., do not cause significant measurement error when using the methoddescribed herein.

FIG. 3 shows an optical schematic of a desired variation of theinventive device. ATR crystal (104) with sample side (114) is shown andIR source (160) is provided. IR source (160) may be any of a variety ofdifferent kinds of sources. It may be a broadband IR source, one havingradiant temperatures of 300° C. to 800° C., or a pair of IR lasersselected for the two regions of measurement discussed above, or othersuitably emitted or filtered IR light sources. A single laser may not bea preferred light source in that a laser is a single wavelength sourceand the preferred operation of this device requires light sourcessimultaneously emitting two IR wavelengths. Lens (162), for focusinglight from IR source (160) into ATR plate (104), is also shown. It maybedesirable to include an additional mirror (163) to intercept a portionof the beam before it enters the ATR plate (104) and then to measure thestrength of that beam in IR sensor (165). Measurement of that incidentlight strength (during normalization and during the sample measurement)assures that any changes in that value can be compensated for.

The light then passes into ATR plate (104) for contact with body part(164), shown in this instance to be the desired finger. The reflectedbeam (106) exits ATR plate (104) and is then desirably split using beamsplitter (166). Beam splitter (166) simply transmits some portion of thelight through the splitter and reflects the remainder. The two beams maythen be passed through, respectively, lenses (168) and (170). Theso-focussed beams are then passed to a pair of sensors which arespecifically selected for detecting and measuring the magnitude of thetwo beams in the selected IR regions. Generally, the sensors will bemade up of filters (172) and (174) with light sensors (176) and (178)behind. Generally, one of the filters (172), (174) will be in the regionof the referencing wavelength and the other will be in that of themeasuring wavelength.

FIG. 4 shows perhaps a variation of this device (200) showing the fingerof the user (202) over the ATR plate (204) with a display (206). Furthershown in this desirable variation (200) is a pressure maintainingcomponent (208). We have found that is very highly desirable to maintaina minimum threshold pressure on the body part which is to be used as thearea to be measured. Generally, a variance in the pressure does notshift the position of the detected IR spectra, but it may affect thesensitivity of the overall device. Although it is possible to teach theuser to press hard enough on the device to reach the minimum thresholdpressure, we have determined for each design of the device it is muchmore appropriate that the design of a particular variation of theinventive device be designed with a specific sample pressure in mind.The appropriate pressure will vary with, e.g., the size of the ATR plateand the like. A constant pressure above that minimum threshold value ismost desired.

The variation shown in FIG. 4 uses a simple component arm (208) tomaintain pressure of the finger (202) on ATR plate (204). Othervariations within the scope of this invention may include clamps and thelike.

It should be apparent that once an appropriate pressure is determinedfor a specific design, the inventive device may include a pressuresensor, e.g., (210) as is shown in FIG. 4, to measure adherence to thatminimum pressure. Pressure sensor (210) may alternatively be placedbeneath ATR plate (204). It is envisioned that normally a pressuresensor such as (210) would provide an output signal which would providea “no-go/go” type of signal to the user.

Further, as shown in FIG. 5, the appropriate pressure may be achievedwhen using our device simply by increasing the pressure of the body parton the ATR crystal surface until a selected, measured IR value becomesconstant.

Method of Use

In general, the inventive device described above is used in thefollowing manner: a skin surface on a human being, for instance, theskin of the finger, is placed on the ATR plate. The skin surface isradiated with an IR beam having components at least in the two IRregions we describe above as the “referencing wavelength” and the“measuring wavelength.” The beam which ultimately is reflected out ofthe ATR plate then contains information indicative of the blood glucoselevel in the user. As noted above, it is also desirable to maintain thatskin surface on the ATR plate at a relatively constant pressure that istypically above a selected minimum pressure. This may be done manuallyor by measuring and maintaining the pressure or monitoring the constancyof a selected IR value.

Typically, the beam leaving the ATR plate is split using an optical beamsplitter into at least two beams. Each of the two beams may be thenfocussed onto its own IR sensor. Each such IR sensor has a specificfilter. This is to say that, for instance, one IR sensor may have afilter which removes all light which is not in the region of thereferencing wavelength and the other IR sensor would have a filter whichremove all wavelengths other than those in the region of the measuringwavelength. As noted above, for glucose, the referencing wavelength istypically in the range of about 8.25 to 8.75 micrometers. For glucose,the measuring wavelength is typically between about 9.5 and 10.0micrometers.

Other analyte materials which have both referencing wavelengths andmeasuring wavelengths in the mid-IR range and that are found in theouter regions of the skin may also be measured using the inventivedevices and procedures described herein.

Respective signals may be compared using analog or digital computerdevices. The signals are then used to calculate analyte values such asblood glucose concentration using various stored calibration values,typically those which are discussed below. The resulting calculatedvalues may then be displayed.

As noted above, it is also desirable both to clean the plate before useand to clean the exterior surface of the skin to be sampled. Again, wehave found, for instance in the early morning that the exterior skin ishighly loaded with glucose which is easily removed preferably by usingthe skin preparation kit, or, less preferably, by washing the hands.Reproducible and accurate glucose measurements may then be had in aperiod as short as ten minutes after cleaning the area of the skin to bemeasured.

We also note that, depending upon the design of a specific variation ofa device made according to the invention, periodic at least an initialcalibration of the device, using typical blood sample glucosedeterminations, may be necessary or desirable.

Determination of blood glucose level from the information provided inthe IR spectra is straightforward. A baseline is first determined bymeasuring the level of infrared absorbance at the measuring andreferencing wavelengths, without a sample being present on the sampleplate. The skin is then placed in contact with the ATR plate and the twospecified absorbance values are again measured. Using these four values,the following calculation is then made.$A_{1} = {{\ln \left( \frac{T_{01}}{T_{1}} \right)} = {A_{g1} + A_{b1}}}$

(Absorbance at referencing spectral band.)$A_{2} = {{\ln \left( \frac{T_{02}}{T_{2}} \right)} = {A_{g2} + A_{b2}}}$

(Absorbance at measuring spectral band.)

where: T₀₁=measured value at reference spectral band w/o sample

T₀₂=measured value at measuring spectral band w/o sample

T₁=measured value at reference spectral band w/sample

T₂=measured value at measuring spectral band w/sample

A_(g1)=absorbance of glucose at reference spectral band

A_(g2)=absorbance of glucose at measuring spectral band

A_(b1)=absorbance of background at reference spectral band

A_(b2)=absorbance of background at measuring spectral band

d=effective path length through the sample.

a₂=specific absorptivity at measuring spectral band

k=calibration constant for the device

C_(g)=measured concentration of glucose

Since the background base values are approximately equal (i.e.,A_(b1)=A_(b2)) and A_(g1)=0, then:

A ₂ −A ₁ =A _(g2) =a ₂ dC _(g)

and

C _(g) =k(A ₂ −A ₁)

The value of C_(g) is the desired result of this procedure.

Similarly, FIG. 7 shows a graph in which the value of the analyte isassessed using similar calculations but in which the “referencingwavelength” is an absorbance trough (“b”) unaffected by theconcentration of the analyte. The “measuring wavelength” peak (“a”) ismeasured against a baseline.

EXAMPLES Example 1

Using a commercially available IR spectrometer (Nicolet 510) having aZnSe crystal ATR plate (55 mm long, 10 mm wide, and 4 mm thick) wetested the inventive procedure. We calibrated the output of thespectrometer by comparing the IR signal to the values actually measuredusing one of the inventor's blood samples. The inventor used a bloodstick known as “Whisper Soft” by Amira Medical Co. and “GlucometerElite” blood glucose test strips sold by Bayer Corp. of Elkhart, Ind. Oneach of the various test days, the inventor took several test sticks andmeasured the glucose value of the resulting blood; the IR test was madeat the same approximate time.

As shown in the calibration curve of FIG. 6, the data are quiteconsistent. So, where the blood glucose concentration “B” is in (mg/dl)and “S” is the difference between the absorbance at the referencingregion and the measuring region as measured by the spectrometer:

B=[(1950)•S]−(17).

Example 2

In accordance with a clinical protocol, a diabetic was then tested.Curve 1 in FIG. 8 shows the IR absorbance spectrum of the test subject'sfinger before eating (and after fasting overnight) and curve 2 shows IRabsorbance spectrum of the same individual after having eaten.Incidentally, insulin was administered shortly after the measurement ofcurve 2.

In any event, the significant difference in the two peak heights at the9.75 micrometer wavelength and the equality of the two IR absorbancevalues at the 8.50 micrometer value shows the effectiveness of theprocedure in measuring glucose level.

Example 3

That the inventive glucose monitoring device non-invasively determinesblood glucose level and quickly follows changes in that blood glucoselevel is shown in FIG. 9. Using both the inventive procedure and acommercial glucose device, one of the inventors followed his glucoselevel for a single day. The blood sticks are considered to be accuratewithin 15% of the actual reading.

The results are shown in FIG. 9. Of particular interest is themeasurement just before 4:40 pm wherein the two values are essentiallythe same. A high sugar candy bar was eaten at about 4:45 pm andmeasurements of glucose level were taken using the inventive procedureat about 5:03, 5:18, 5:35 and 5:50. A blood sample was taken at 5:35 andreflected almost the same value as that measured using the inventiveprocedure. Consequently, the procedure tracks that measured by the bloodvery quickly.

This invention has been described and specific examples of the inventionhave been portrayed. The use of those specifics is not intended to limitthe invention in any way. Additionally, to the extent there arevariations of the invention with are within the spirit of the disclosureand yet are equivalent to the inventions found in the claims, it is ourintent that this patent will cover those variations as well.

We claim as our invention:
 1. A method for determining a blood glucoselevel of a human being through contact with a skin surface, comprisingthe acts of: a.) wiping the skin surface with a glucose solvent, b.)removing the glucose solvent from the skin surface, c.) irradiating saidskin surface with light containing at least an IR component so toproduce a reflected IR beam indicative of said blood glucose level, d.)detecting said reflected R beam, and e.) calculating the glucose levelfrom said reflected IR beam.
 2. The method of claim 1, includingrepeating acts c.), d.) and e.) until a consistent glucose level readingis obtained.
 3. The method of claim 1, wherein said IR componentcontains mid-IR wavelengths.
 4. The method of claim 1, wherein saidsolvent is a highly polar solvent.
 5. The method of claim 1, whereinsaid act of wiping further comprises wiping with a for removingsaid-solvent.
 6. The method of claim 1, wherein said solvent has an IRspectra different from an IR spectra of glucose.
 7. The method of claim1, further comprising an act of maintaining said skin surface against anATR plate at an adequate pressure during the act of irradiating saidskin surface with light containing at least an IR component so toproduce a reflected IR beam indicative of said blood glucose level. 8.The method of claim 1, wherein said IR component further comprises areferencing wavelength and a measuring wavelength.
 9. The method ofclaim 8, wherein said referencing wavelength is between about 8.25 μmand about 8.75 μm.
 10. The method of claim 8, wherein said measuringwavelength is between about 9.50 μm and about 10.00 μm.
 11. The methodof claim 8, wherein said act of calculating the glucose level comprisescomparing an absorbance of said reflected IR beam at said referencingwavelength and said measuring wavelength.
 12. The method of claim 1,wherein said act of detecting further comprises an act of absorbing saidreflected IR beam with at least two IR sensors.